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Allopurinol

NDC 71921-240 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerFlorida Pharmaceutical Products, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA204467
Dosage form / routeTABLET · ORAL
Active ingredientsALLOPURINOL (100 mg/1)
Marketing started20231031
Package count4

External sources

Source: openFDA. Public-domain (CC0).